Figure 1
Figure 1. Characteristics of post-dUCBT patient PBMC samples before and after HLA class II allele-specific T-cell propagation. (A) Absolute numbers of CD3+ T cells in PB samples analyzed for HLA class II allele immune recognition. Graphs represent individual and median (line) values. Dotted line, lower limit of normal values of CD3+ T cells in blood of healthy individuals. (B) Percentage of CD4+ T cells in PB (before) and in T-cell cultures after HLA class II–specific amplification, with either HeLa cells transduced with HLA class II mismatched alleles (after, MM) or with HLA class II third-party alleles (after, 3P). Depending on the number of mismatched alleles in the dUCBT combination, from 1 to 7 T-cell amplification cultures per PB sample were performed. Graphs represent individual and median (line) observations. Gray area, normal range of CD3+CD4+ values in blood of healthy individuals; significance in nonpaired t tests is shown. (C) Increase in T-cell numbers in post-dUCBT PBMC samples following processing in HLA class II–specific amplification cultures, expressed as fold increase relative to the T-cell number at start of culture (see B).

Characteristics of post-dUCBT patient PBMC samples before and after HLA class II allele-specific T-cell propagation. (A) Absolute numbers of CD3+ T cells in PB samples analyzed for HLA class II allele immune recognition. Graphs represent individual and median (line) values. Dotted line, lower limit of normal values of CD3+ T cells in blood of healthy individuals. (B) Percentage of CD4+ T cells in PB (before) and in T-cell cultures after HLA class II–specific amplification, with either HeLa cells transduced with HLA class II mismatched alleles (after, MM) or with HLA class II third-party alleles (after, 3P). Depending on the number of mismatched alleles in the dUCBT combination, from 1 to 7 T-cell amplification cultures per PB sample were performed. Graphs represent individual and median (line) observations. Gray area, normal range of CD3+CD4+ values in blood of healthy individuals; significance in nonpaired t tests is shown. (C) Increase in T-cell numbers in post-dUCBT PBMC samples following processing in HLA class II–specific amplification cultures, expressed as fold increase relative to the T-cell number at start of culture (see B).

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